rs1057518628
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs1057518628(-;-) |
Make rs1057518628(-;C) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | X |
Position | 136659107 |
Gene | CD40LG |
is a | snp |
is | mentioned by |
dbSNP | rs1057518628 |
dbSNP (classic) | rs1057518628 |
ClinGen | rs1057518628 |
ebi | rs1057518628 |
HLI | rs1057518628 |
Exac | rs1057518628 |
Gnomad | rs1057518628 |
Varsome | rs1057518628 |
LitVar | rs1057518628 |
Map | rs1057518628 |
PheGenI | rs1057518628 |
Biobank | rs1057518628 |
1000 genomes | rs1057518628 |
hgdp | rs1057518628 |
ensembl | rs1057518628 |
geneview | rs1057518628 |
scholar | rs1057518628 |
rs1057518628 | |
pharmgkb | rs1057518628 |
gwascentral | rs1057518628 |
openSNP | rs1057518628 |
23andMe | rs1057518628 |
SNPshot | rs1057518628 |
SNPdbe | rs1057518628 |
MSV3d | rs1057518628 |
GWAS Ctlg | rs1057518628 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs1057518628(-;-) |
Alt | rs1057518628(-;-) |
Reference | Rs1057518628(C;C) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | CD40LG |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000023.10:g.135741266delC |
CLNSRC | |
CLNACC | RCV000414255.1, |